78795
N-Phenylmaleimide
≥98.0% (HPLC)
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About This Item
Empirical Formula (Hill Notation):
C10H7NO2
CAS Number:
Molecular Weight:
173.17
EC Number:
213-382-0
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
125098
MDL number:
assay
≥98.0% (HPLC)
bp
162-163 °C/12 mmHg (lit.)
mp
85-87 °C (lit.), 89-90 °C
SMILES string
O=C1C=CC(=O)N1c2ccccc2
InChI
1S/C10H7NO2/c12-9-6-7-10(13)11(9)8-4-2-1-3-5-8/h1-7H
InChI key
HIDBROSJWZYGSZ-UHFFFAOYSA-N
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Aquatic Acute 1
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Regulatory Information
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Jian-Hui Wen et al.
Talanta, 84(1), 13-18 (2011-02-15)
Representing a compound by a numerous structural descriptors becomes common in quantitative structure-activity relationship (QSAR) studies. As every descriptor carries molecular structure information more or less, it seems more advisable to investigate all the possible descriptor vectors rather than traditional
Stewart F Parker
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 63(3), 544-549 (2005-09-15)
A combination of infrared, Raman and inelastic neutron scattering (INS) spectroscopies with density functional theory (DFT) calculations is used to provide a complete assignment of the vibrational spectra of N-phenylmaleimide and N-(perdeuterophenyl)maleimide. DFT is shown to give very good results
Vânia F Noldin et al.
Pharmacological reports : PR, 63(3), 772-780 (2011-08-23)
Myeloperoxidase (MPO) is an important enzyme that catalyzes the reaction between hydrogen peroxide and chloride to generate hypochlorous acid, which oxidizes a range of biomolecules and has been associated with inflammatory diseases. The synthetic compounds N-phenylmaleimide (NFM) and 4-methyl-N-phenylmaleimide (Me-NFM)
I Velasco-Guillén et al.
Archives of biochemistry and biophysics, 372(1), 121-127 (1999-11-24)
The Ca(2+)-ATPase from sarcoplasmic reticulum reacts with phenylmaleimide, producing the inhibition of the ATPase activity following a pseudo-first-order kinetic with a rate constant of 19 M(-1) s(-1). Calcium and ATP binding are not altered upon phenylmaleimide inhibition. However, the presence
Yan Wang et al.
The Journal of organic chemistry, 77(8), 4143-4147 (2012-04-05)
A Me-DuPhos-catalyzed efficient asymmetric [3 + 2] cycloaddition reaction between Morita-Baylis-Hillman carbonates of isatins and N-phenylmaleimide has been developed. This reaction constructs three chiral centers in one step to afford spirocyclopentaneoxindoles in good yields (up to 84%) with excellent diastereo-
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 8212581000 | 04022536476902 |
| 464953-90L | 04061838111302 |
| 464953-400L | 04061837457180 |
| 59240-1ML-F | 04061837781469 |
| 59240-10ML-F | 04061837781452 |
| I19551-18L-KL | 04061837329982 |
| I19551-100ML | 04061833848227 |
| 8212580100 | 04022536476896 |
| I19551-500ML | 04061837329999 |
| I19551-PZ | 04061822597631 |
| 464953-PZ | 04061837457203 |
| 464953-200L | 04061838220035 |
| 464953-200L-DR | 04061837457173 |
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